HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1380Generated: October 26, 2026
Triisopropyl borate → (5,6,7,8-Tetrahydro-5,5-dimethylnaphth-2-yl)boronic acid
https://huagongshe.com/reaction/1380
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triisopropyl borate | HCID 21531 | — |
| Reactant | 6-Bromo-1,1-dimethyl-1,2,3,4-tetrahydronaphthalene | HCID 10586063 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | (5,6,7,8-Tetrahydro-5,5-dimethylnaphth-2-yl)boronic acid | HCID 22571498 | — |
Reaction Steps
To a cold (-78° C.) solution of 2.02 g (8.4 mmol) of 6-bromo-1,2,3,4-tetrahydro-1,1-dimethylnaphthalene in 11.0 mL of toluene, was added 4.6 g (6.8 mL, 10.9 mmol, 1.6M in hexane) of n-BuLi. The resulting solution was stirred at -78° C. for 45 min. and then 2.40 g (3.0 mL, 12.7 mmol) of triisopropylborate was dropwise added and the reaction stirred at room temperature for 12 h. The reaction was then diluted with 10% HCl, and extracted with ether (2×). The combined organic layer was washed with brine, dried over MgSO4, and concentrated in vacuo to give an oil. Recrystallization from hexane afforded the title compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05723666 |
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| Source dataset | uspto-grants-1998_03 |
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| ORD ID | ord-1def6f145a124de08c583f52bfc46d3d |
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| Source note | uspto-grants-1998_03 |
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